Canonical Allele Identifier: PA2829069929
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11831
ClinVar RCV Id: RCV000012604 RCV000132982 RCV001719695 RCV002260597 RCV002371770 RCV004540997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Gly205Ser
CA121707
NM_001386139.1:c.613G>A